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Job DescriptionJob DescriptionThe Medidata Rave Study Builder will be responsible for creating Rave studies for therapeutic oncology trials. Incumbent will bring experience with study build activities in Medidata Rave, preferably in oncology.
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Assisting as necessary with the internal GLP activities to conform with the GLP regulations (21 CFR Part 58) across the Medical Device CommunityMaintaining a copy of a master schedule sheet of all nonclinical laboratory studies conducted at Ethicon indexed by test article and containing the test system, nature of study, date study was initiated, current status of each study, identity of the sponsor, and name of the study director.
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The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.
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Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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The#Protocol Review and Regulatory Affairs department is looking for a Regulatory Startup Project Coordinator Summary: The Regulatory Startup Project Coordinator is responsible for shepherding clinical research projects through the study start up process to ensure activation time-lines meet (or exceed) institutional standards.
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Payment options: GoGift Cards paid on the day after the study is completed or Hyperwallet (through TELUS International AI Community Platform) – payments will be processed and paid out a couple of weeks after the study is completed.
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The Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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SIT Study Abroad offers accredited summer and semester undergraduate programs in Africa, Asia and the Pacific, Europe, Latin America, and the Middle East, as well as comparative programs on multiple continents.
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Use databases for animal recordkeeping, including but not limited to, animal housing and study support. The Vivarium at Janelia is an AAALAC accredited facility that supports ground-breaking research in a variety of animal models (currently with a focus on mice, rats, and zebrafish) and is one of the highest regarded in the world.
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Expertise in more than one area of study or research, e.g., pharmacology, pharmacodynamics, pharmacogenomics. General Information: Manchester University is an independent, liberal arts university with a campus in North Manchester, Ind., where approximately 1,300 students choose from at least 60 areas of undergraduate study, master's programs, and 21 NCAA Division III varsity sports.
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The goals of the Home-Study Post Release Services Program (HS/PRS) are to: Assess the safety and suitability of a sponsor before an unaccompanied child is released from custody into a sponsor's care (Home Study) Provide case management support via remote and / or conducting in-home visits to ensure the continued safety and stability of children in sponsor's homes and linking children to resources in the community (Post Release Services.
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Clinical Research Coordinator for Large Neuroimaging Study of Aging and Alzheimer’s disease. The Mormino Laboratory within the Department of Neurology and Neurological Sciences is seeking a Clinical Research Coordinator Associates (CRCA) to work on a biofluid-imaging study focused understand human aging and Alzheimer’s disease (the Stanford Aging and Memory Study, SAMS.
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Significant experience as study director or study monitor conducting nonclinical in vitro and in vivo toxicity studies using various exposure scenarios with demonstrated progression to roles of increasing responsibility and breadth (e.g., study monitor/director to tox program manager, etc.
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The Sr. Clinical Data Manager will be responsible to support all aspects of data management from study start-up to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer specifications.
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Our BA, BFA, MA, MFA, PhD, and DSC programs offer the most rigorous study in the study and practice of media and the communication arts in all forms. Equipped with a $35 million Communication & Performing Arts Center, this state-of-the-art school produces over 100 student films annually and has won over 700 local, national, and international student film awards.
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